Literature DB >> 11121492

TE-AFLP: combining rapidity and robustness in DNA fingerprinting.

A W van Der Wurff1, Y L Chan, N M van Straalen, J Schouten.   

Abstract

A new type of fingerprinting technique is presented, based on amplified fragment length polymorphism (AFLP). Rather than two endonucleases as in AFLP, we propose the use of three enzymes, hence the method is called three endonuclease (TE)-AFLP. Genomic DNA is digested and two sets of adapters are selectively ligated onto the restriction fragments in a single reaction volume. No adapters complementary to the ends generated by a frequent cutter are added. Due to the addition of a third endonuclease, the TE-AFLP method provides a high discriminatory power and a reduction in the number of bands. The latter makes it especially suitable for the analysis of complex genomes. TE-AFLP fingerprints are suitable for detection by automatic fluorescent sequencers and are obtained in less than half the time and at reduced costs compared to a typical AFLP. The reliability of this method was investigated by determining the influence of varying digestion, ligation and PCR components on the fingerprint. Moreover, cross-experiments to study inheritance of loci were performed with a primitive insect and with tomato strains. The features of TE-AFLP are discussed in comparison with conventional AFLP.

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Year:  2000        PMID: 11121492      PMCID: PMC115249          DOI: 10.1093/nar/28.24.e105

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  9 in total

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7.  Multicolour fluorescent detection and mapping of AFLP markers in chicken (Gallus domesticus).

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  9 in total
  14 in total

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9.  Quantitative oligonucleotide microarray fingerprinting of Salmonella enterica isolates.

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